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Results of search for 'au:"H'mida, D"'
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Authors
Adala, L
Al-Rayess, M
Almubarak, M
Anheim, M
Bétard, C
Chaieb, A
Drouot, N
Elghezal, H
Elmalik, S
Goebel, H
Gribaa, M
H'mida, D
Kabiraj, M
Koenig, M
Lagier-Tourenne, C
Mohamed, A
Saad, A
Salih, M
Yacoubi, T
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Topics
Adolescent
Adult
Androgens
Beckwith-Wiedemann Syndrome
Biopsy
Brain
Cell Line
Child
Child, Preschool
Chimerism
Chromosome Mapping
Chromosomes, Human, Pair 16
Electroencephalography
Epilepsy, Tonic-Clonic
Female
Fetus
Genotype
Homozygote
Humans
pathology
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English
Your search returned 2 results.
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1.
Placental mesenchymal dysplasia with beckwith-wiedemann syndrome fetus in the context of biparental and androgenic cell lines.
[electronic resource]
by
H'mida, D
Gribaa, M
Yacoubi, T
Chaieb, A
Adala, L
Elghezal, H
Saad, A
Producer:
20080825
In:
Placenta
vol. 29
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Available from publisher's website
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2.
A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23.
[electronic resource]
by
Gribaa, M
Salih, M
Anheim, M
Lagier-Tourenne, C
H'mida, D
Drouot, N
Mohamed, A
Elmalik, S
Kabiraj, M
Al-Rayess, M
Almubarak, M
Bétard, C
Goebel, H
Koenig, M
Producer:
20070724
In:
Brain : a journal of neurology
vol. 130
Online resources:
Available from publisher's website
Availability:
No items available.
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